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Granulomatosis With Polyangiitis

Disease ID: disease_node_7959

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DbxrefGARD:7880, ICD10CM:M31.3, ICD9CM:446.4, MESH:D014890, MIM:608710, NCI:C3444, SNOMEDCT_US_2023_03_01:195353004, UMLS_CUI:C3495801
SubclassofDOID_557, DOID_850, DOID_37, DOID_0060050
Data SourceDOID, MESH
SynonymsNecrotizing respiratory granulomatosis, Wegener granulomatosis, formerly
Disease Has LocationUBERON_0002113, UBERON_0000014, UBERON_0002048, UBERON_0000178
Mesh IdD014890
Mesh LabelGranulomatosis with Polyangiitis
Mesh SubclassofD017563, D056648
Doid Labelgranulomatosis with polyangiitis
Doid DescriptionAn autoimmune disease that is characterized by necrotizing granulomatous inflammation of the upper and lower respiratory tract, glomerulonephritis, vasculitis, and the presence of antineutrophil cytoplasmatic autoantibodies (ANCAs) in patient sera, and is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels.
Has SymptomSYMP_0000709, SYMP_0000153
Disease Node Iddisease_node_7959
Doid IdDOID_12132
LabelGranulomatosis With Polyangiitis